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Old 02-11-2010, 09:39 PM
keep smilin keep smilin is offline
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Join Date: Aug 2009
Posts: 851
15 yr Member
keep smilin keep smilin is offline
Member
 
Join Date: Aug 2009
Posts: 851
15 yr Member
Heart Okay..let me say.....

Quote:
Originally Posted by loretta View Post
Hi Momof4, I totally agree with Sandy on the SCS. I also have generalized RSD full body SIP. My Dr. is a neurologist, psychiatrist, and pharmacologist. He is very conservative and I have been seeing him 6th year. He is against Methadone. I have been taking vicodin for years. About 6 months ago I was able to go down from 6 a day to 4 . My Dr. believes in muli meds to minimize the opiads. I also take Lorazepam also reduced from 6 to 4. I take 2 blood pressure meds. Cymbalta 120 mg. and a sleeping pill. I used to take 3200 mg neurotin but was able to slowly go off and the electric jerk and jolts did not come thru. I hated that med-weight gain. I have a window of time to drive. I am totally mobile with the exception of one hand 50% range of motion. It was 4 years before I was diagnosed and had delay of treatment of the hand.
I did go thru 150 physical therapy treatments for both frozen shoulders, but got full range of motion back- that was before diagnosis of RSD. I had a year remission after each shoulder
My third round with RSD came while water skiing. I pulled a nerve in one hand getting up out of the water. Misdianosed as RA- Changed Drs. and diagnosed with RSD in one min. confirmed with nuclear med. equipment.
My Dr. just built two clinics with HBOT and I'm going to try the HBOT. I also have trigeminal nerve disorder-feels like an ice pick in temple. loss of feeling down left side of face. I also have internal pelvic RSD If the HBOT doesn't work, I'll consider Ketamine.
How are you doing? I was devasted when a new neuro said I had generalized. He suggested seeing a psychiatrist. I didn't like his two suggestions, in fact I didn't like him. So I found one on my own. The first visit I knew he could help me. He is a gem. I had already had over 2 years of counseling with a psychologist when my parents died. and that helped. but as we both know, this is a different animal.
Are you mobile? have you had pt. I found massage therapy very good. I started right away. and had it each time just before the pt. This is all before I was diagnosed with RSD. Now, I find swimming pool 86 degrees, very helpful in keep mobile and even reversing my toes that were curling. They went back to touching the floor in 4 months in the pool.
Really hope the best for you. please let us know how you are doing? Your friend, loretta with soft hugs
As we are all aware... not one treatment or medicine works the same for any of us..so who is to know what affect we'll all get..there now with that said...

We go thru the high and lows of treatment and interventions...SCS, blocks..Ketamine...on and on... I am beginning to feel a bit like the fury fella running on the wheel..anyone else???? I am starting to side with one of our friends who once said..I am done..DONE.. done..with it all..I am an RSD mess and that is the way I will live... one good thing..we won't die from it...thats what they say right???

Guess I am sounding tired..but what I really want to say is..I wish I had a magic wand..cuz if I did ..I would love to make you all here feel better and rid of your RSD....

Momf4... I am so sorry on what you should really do...as it seems we are all hitting the part in the road in which way to turn.. Our Dr.'s still go home at night ... painfree themselves..leaving us lie awake at night wondering what tomorrow has in store for us.. Please let us know how you are doing.. We are your friends....

You, and all of my friends here are in my prayers....

Kathy
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RNcrps2 (02-12-2010), SandyRI (02-12-2010), SandyS (02-11-2010)